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Balancing the Acute Phase Response during the Transition Period: Impacts on Performance and Health

Published: June 11, 2012
By: Barry Bradford (Kansas State University)
Introduction
The multitude of disorders that dairy cows face during the transition to lactation is a perennial source of concern for dairy producers, nutritionists, and veterinarians. Total disease incidence in the several weeks after parturition accounts for a substantial proportion of all morbidity on many dairies, with particularly high rates of mastitis, metritis, milk fever, displaced abomasum, ketosis, and fatty liver, among other problems. Not surprisingly, these issues have been the focus of much research in recent decades. During that time, substantial progress has been made in some areas (e.g. milk fever); however, incidence of other disorders (e.g. displaced abomasum) may be on the rise (Goff, 2006).
Recent research has highlighted the role of inflammation in infectious diseases and has suggested that inflammation is involved in metabolic diseases as well. A key role for inflammation in numerous transition cow disorders may help to explain links between these diverse conditions. On the other hand, inflammatory pathways play important roles in normal immune function, metabolism, and reproduction. An improved understanding of the necessary and pathological aspects of inflammatory pathways in transition cows may improve our ability to predict and prevent transition disorders.
Inflammation and the Acute Phase Response
During infections such as mastitis or metritis, immune cells in the body recognize invading pathogens and become activated. When the infection is caused by Gramnegative bacteria, lipopolysaccharide (LPS) released by the bacteria also activates immune cells. The activation of local and systemic host defense mechanisms requires cross-talk between numerous types of immune cells, and one component of this response is inflammation. The host of signaling molecules released by activated immune cells includes inflammatory mediators such as nitric oxide, prostaglandins, and cytokines. While many of these molecules promote local inflammation and increased blood flow to the infected tissue, inflammatory cytokines play a key role in stimulating systemic inflammatory responses, including increased body temperature, increased heart rate, and decreased feed intake (Dantzer and Kelley, 2007). Cytokines are able to alter many physiological systems because nearly all cell types express cytokine receptors. Key inflammatory cytokines include tumor necrosis factor alpha (TNFα), interleukin (IL) 1β, and IL-6; these inflammatory cytokines act through many of the same signaling cascades and often produce similar responses in cells.
One effect of cytokines is to activate production of acute phase proteins. Primarily produced by the liver, this class of proteins includes haptoglobin, serum amyloid A, and C-reactive protein. Proteins that participate in the acute phase response to infection are generally found in very low abundance in the bloodstream, but are greatly elevated during systemic activation of the immune system. The importance of acute phase proteins in the response to infection is somewhat unclear, but they have gained widespread acceptance as markers of inflammation.
It is clear that mammary and uterine infections result in both local and systemic inflammation. Coliform mastitis results in release of LPS into the bloodstream and increased plasma concentrations of cytokines and acute phase proteins (Hoeben et al., 2000). Likewise, metritis is associated with an acute phase response in transition cows (Huzzey et al., 2009); in fact, plasma haptoglobin is elevated prior to clinical signs of metritis. Furthermore, monocytes are known to become more responsive to inflammatory stimulants during the transition period, resulting in greater secretion of inflammatory cytokines when stimulated (Sordillo et al., 1995). Mastitis and metritis can therefore result in systemic inflammation.
Is There a Role for Inflammation in Metabolic Disorders?
Inflammation has been proposed as a missing link in the pathology of metabolic disorders in transition cows (Drackley, 1999). Recent findings have documented relationships between inflammatory mediators and metabolic disorders. Plasma concentrations of haptoglobin and serum amyloid A were increased in cows that developed fatty liver (Ametaj et al., 2005), and Ohtsuka and colleagues (2001) observed increased serum TNFα activity in cows with moderate to severe fatty liver. A retrospective study of cows on 3 commercial Italian dairies suggested that liver inflammation is associated with a problematic transition to lactation (Bertoni et al., 2008). Cows were classified in quartiles for degree of liver inflammation based on plasma concentrations of acute phase proteins. Those cows with the strongest inflammatory profiles were at 8-fold greater risk for experiencing one or more transition disorders, had lower plasma calcium concentrations, took longer to re-breed, and produced less milk in the first month of lactation (Bertoni et al., 2008). These correlations have driven strong interest in potential mechanisms underlying an inflammation-based pathogenesis of transition cow disorders.
Strong evidence has emerged from 2 recent studies where inflammatory mediators directly induced metabolic problems. Trevisi and colleagues (2009) orally administered interferon-α (a cytokine) daily during the final 2 weeks of gestation, which caused liver inflammation and release of acute phase proteins. Compared to control cows, treated cows had significantly higher plasma ketone concentrations in the first 2 weeks after calving. Our own lab recently reported that subcutaneous injection of TNFα for 7 days doubled liver triglyceride content in late-lactation dairy cows (Bradford et al., 2009). We also observed changes in mRNA abundance consistent with transcriptionally-mediated increases in fatty acid uptake and esterification and decreased fatty acid oxidation. These results strongly support the hypothesis that inflammation disrupts normal metabolism, because although both of the above treatments were considered low-dose and short-term, they nevertheless promoted ketosis and fatty liver, respectively.
Beyond direct promotion of ketosis and fatty liver, hepatic inflammation may also impair glucose production. Endotoxin-induced mastitis was shown to alter expression of metabolic genes in the liver, including decreased expression of genes important for glucose production (Jiang et al., 2008). Our TNFα injection protocol also decreased expression of several of the same glucose synthesis genes (Bradford et al., 2009). In early lactation cows, impaired glucose production would likely lead to increased adipose tissue breakdown, elevated plasma NEFA, and increased ketone production by the liver.
Relationships between Oxidative Stress and Inflammation
Although the importance of inflammation in transition disorders is becoming clear, the pathways that cause this inflammation are less clear. Infections certainly initiate the process in some cows, but this is not likely the cause of metabolic disorders in all cows. In particular, the dramatically higher incidence of transition disorders in cows with excessive body condition is difficult to attribute exclusively to infections. Lipid peroxides are emerging as likely mediators linking plasma lipids to inflammation.
Lipid peroxides are produced when intracellular lipids encounter reactive oxygen species (ROS) such as hydrogen peroxide. Some ROS are always produced in the liver; however, events occurring in early lactation likely contribute to enhanced ROS production. One adaptation to increasing delivery of NEFA to the liver in early lactation is an increase in the capacity of peroxisomal oxidation (Grum et al., 1996), an alternative pathway for fatty acid oxidation. Enhanced peroxisomal oxidation increases total oxidative capacity of the cell, but the first step in this pathway produces hydrogen peroxide rather than NADH (Drackley, 1999), and therefore it contributes to ROS production to a greater extent than mitochondrial oxidation.
Increased ROS production in early lactation cows, coupled with increased NEFA concentration, increases lipid peroxide formation; both the transition to lactation and high body condition are associated with increased plasma markers of lipid peroxidation (Bernabucci et al., 2005). Lipid peroxides activate inflammatory cascades, which in turn alter nutrient metabolism. In addition, ROS are especially harmful to immune cells and can decrease the ability of the immune system to respond to infections (Spears and Weiss, 2008).
Requirements for Inflammatory Pathways in the Transition Cow
Although the term "inflammation" conjures thoughts of pain and disease, inflammatory pathways and compounds are critical to many aspects of physiology. In many cases, activation of inflammatory pathways promotes resolution of problems, even those that do not result in apparent disease. During infections, inflammatory signals promote activation and recruitment of immune cells, increasing the delivery of cells that can engulf bacteria, produce extracellular traps, and increase blood flow to the site of infection. Even in conditions that don´t involve pathogens, inflammatory pathways can be beneficial. For example, if a liver cell dies, the cellular contents that are released can activate inflammatory pathways in neighboring cells. If the situation is mild, this triggers the cell to turn on protective machinery to aid the cell´s ability to survive a cytotoxic challenge. Without this inflammatory response, minor problems that cause cell death could rapidly spiral into broad tissue necrosis (Vainer et al., 2008).
Another critical role of inflammatory pathways in the transition cow is to promote labor and expulsion of the placenta. Like many reproductive processes, signaling molecules known as prostaglandins are critical in this process. Prostaglandin production requires the presence of long-chain polyunsaturated fatty acids as substrates and a number of enzymes, including cyclooxygenase and prostaglandin synthases. Production of prostaglandins can be limited by availability of fatty acid substrates, but is also highly regulated by enzyme activity. The same inflammatory pathways that alter liver function and activate immune cells also stimulate prostaglandin synthesis. This is a critical process in the term fetus, as prostaglandin E2 synthesis in the fetal membranes is thought to act directly on cervical tissue and myometrial cells to dilate the cervix and induce contraction, contributing to the initiation of parturition (Challis et al., 2009).
Perhaps the clearest indication of the mixed benefits and problems associated with inflammation comes from human genetics. Toll-like receptor 4 (TLR4) is a cellular receptor that recognizes bacterial endotoxin and numerous other ligands, and activates inflammatory cascades in response. A relatively common TLR4 mutation discovered in humans decreases the ability of the receptor to activate inflammation. This mutation has been found to decrease the risk of diabetes and its comorbidities (Kolek et al., 2004) but also to increase the risk of clinical infections (Vogel et al., 2005). Balancing inflammation during the transition period may be critical to minimizing overall disease risk during this period.
Potential Interventions
Antioxidants. Dietary antioxidants, notably vitamin E and selenium, are important for their ability to contribute to ROS neutralization, thereby impeding the progression toward inflammation. Interestingly, plasma concentrations of α-tocopherol (vitamin E) decrease through the transition period (Weiss et al., 1990a), and low antioxidant status is associated with transition cow disorders (Mudron et al., 1997, LeBlanc et al., 2004). Supplementing vitamin E prepartum improves antioxidant status (Weiss et al., 1990b). Multiple studies have shown that supplementing vitamin E in excess of traditional recommendations decreases the incidence and severity of clinical mastitis (Smith et al., 1984, Weiss et al., 1990b). Additionally, a meta-analysis showed that supplemental vitamin E is effective at preventing retained placenta (Bourne et al., 2007).
Although much of the literature on antioxidants in transition cows demonstrates positive effects, these nutrients must be used with caution. In an effort to maximize the odds of observing a response, most studies are designed with rather dramatic treatments; for example, the classic Weiss study cited above (1990b) compared vitamin E intakes of 574 IU/day (no supplemental vitamin E) to 1474 IU/day (supplementing 40 IU/kg dry matter). In many such scenarios, the control group is fed a diet that is marginally deficient in the nutrient of interest. On most dairies, this is not the case. As a result, adding large amounts vitamin E, for example, can sometimes push the supply of the nutrient high enough to cause mild toxicity. Supplementing 3000 IU/day vitamin E to transition cows with adequate vitamin E status resulted in pro-oxidant responses, increasing markers of lipid peroxidation and the incidence of mastitis (Bouwstra et al., 2010). Any treatment that alters oxidative balance should be evaluated carefully.
Non-steroidal anti-inflammatory drugs (NSAIDs). Flunixin meglumine was evaluated in 2 recent studies in which transition cows were treated prior to any disease diagnosis to assess whether flunixin might prevent disorders. Shwartz and colleagues (2009) showed no benefit to administration of flunixin meglumine for the first 3 days of lactation. In fact, this treatment depressed feed intake and milk yield over the first week of lactation. In a much larger study, Duffield and coworkers (2009) demonstrated that flunixin injections in the first 2 days postpartum significantly increased the risk of retained placenta and metritis. This negative finding may be due to the ability of flunixin to inhibit cyclooxygenase enzymes, suppressing prostaglandin synthesis and slowing uterine contractions necessary for expulsion of the placenta.
Salicylates have also been evaluated for use in the treatment of mastitis, and in general they are effective at reducing body temperatures, but do not appear to decrease the severity of the infection (Morkoc et al., 1993). However, this class of NSAIDs shows some promise in regard to metabolic inflammation. Cows treated with acetyl-salicylate (aspirin) for the first 5 days of lactation had significantly lower plasma concentrations of acute phase proteins and tended to have greater peak milk production than controls (Bertoni et al., 2004). In a similar study, aspirin treatment for 5 days postpartum improved milk yield in the first 2 months of lactation and increased first service conception rates (Trevisi and Bertoni, 2008). A relatively small number of cows was included in the study (23/treatment); however, ketosis incidence appeared to decrease with aspirin treatment (4.4% vs. 22.7%) while metritis incidence appeared to increase (30.4% vs. 13.6%). Again, these results point to the tradeoffs between metabolic and immune function associated with decreased inflammation.
Omega-3 fatty acids. A class of long-chain fatty acids, omega-3 fatty acids include alpha-linolenic acid, eicosapentaenoic acid, and docosahexaenoic acid. Although these fatty acids are typically found in low abundance in ruminant diets, a number of recent studies have evaluated the use of flaxseed or fish oil-derived products to increase dietary supply of omega-3s. One reason for the interest in these compounds is that they can suppress inflammatory pathways. This effect has traditionally been ascribed to the idea that increasing supply of omega-3 fatty acids decreases the production of inflammatory compounds from omega-6 fatty acids. Recently, a cell surface receptor was characterized that more directly mediates anti-inflammatory effects of omega-3 fatty acids (Oh et al., 2010).
Thatcher and colleagues have attempted to promote immune function in the transition period by supplementing omega-6 fatty acids compared to omega-3 fatty acids, supplied in the form of calcium salts of fatty acids. Although this form of fatty acid protection does not make the fatty acids inert in the rumen, biohydrogenation is slowed enough for these supplements to alter fatty acid composition of tissues. Increasing the ratio of omega-6 to omega-3 fatty acids increased the production of hydrogen peroxide and phagocytosis of bacteria by neutrophils (Thatcher et al., 2010), which could be due to increased supply of omega-6 precursors of inflammatory compounds and/or decreased supply of anti-inflammatory omega-3 fatty acids. This treatment also increased plasma concentrations of 2 acute phase proteins (Thatcher et al., 2010), indicating a more inflamed state of the liver during the transition period. While the observed effects on neutrophil function would be expected to improve the ability of the immune system to ward off infection, liver inflammation is associated with impaired metabolic function (Bertoni et al., 2008, Bradford et al., 2009). Like the other strategies discussed above, the potential benefits of such an approach may depend on the incidence of metabolic vs. infectious diseases on a given farm, the metabolic state of the cows in question, and even the diet to which the fatty acid supplement is added.
Immunomodulary peptides. The next generation of immune modulators may be peptide-based treatments. Peptides designed to mimic endogenous host defense peptides have improved immune response to some pathogenic challenges, and have advantages over antibiotics in terms of their lack of residue in food products as well as consumer acceptability. However, host defense peptides can cause non-specific inflammation and some may not be good tools for use in transition cows. A novel class of small cationic peptides, coined "immunomodulary peptides", were designed to promote immune function without the inflammatory effects of host defense peptides. One such peptide was shown to improve survival of mice exposed to either Gramnegative or Gram-positive pathogens, primarily by increasing the effectiveness of macrophages (Scott et al., 2007). Remarkably, the peptide not only failed to induce nonspecific inflammation, it actually decreased inflammatory responses to LPS in monocytes, decreasing expression of TNFα and IL-6 and increasing IL-10 expression. In the future, technologies promoting improved clearance of pathogens with limited inflammation may help cows to navigate the transition period with lower risk of both infectious and metabolic disease.
Conclusions
In summary, research in the fields of metabolism, reproduction, and immunology are uncovering a growing list of physiological functions influenced by inflammatory pathways. The acute phase response is common in transition cows, indicating the presence of an inflammatory state. While this state can help support the cow´s ability to calve, expel the placenta, and fight off infection, it may also strain the metabolic system that is critical for handling fatty acids mobilized from body stores and providing nutrients to support lactation. Consistent with this idea, various anti-inflammatory strategies have shown promise for minimizing metabolic disease while also increasing the risk of retained placenta and perhaps infection. Striking the right balance between immune responsiveness and inflammation may be critical to reducing transition disorders.
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This paper was presented at the 22nd Annual Florida Ruminant Nutrition Symposium at the Best Western Gateway Grand Hotel, Gainesville, Florida, USA. February 1-2, 2011. Engormix.com thanks the author and the organizing committee for this huge contribution. 
Dr. Barry Bradford completed dual bachelor´s degrees at Iowa State University and a doctorate in animal nutrition at Michigan State University. In 2006, he began his current position as an assistant professor at Kansas State University. Bradford oversees an active research program focused on alternative feedstuffs, transition cow health, and physiological regulation of carbohydrate and lipid metabolism. In addition, he teaches over 150 students per year in several undergraduate and graduate courses in nutrition and physiology.
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Authors:
Barry Bradford
Michigan State University
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